Bevacizumab Treatment for Advanced Breast Cancer

Author:

Alvarez Ricardo H.1,Guarneri Valentina2,Icli Fikri3,Johnston Stephen4,Khayat David5,Loibl Sibylle6,Martin Miguel7,Zielinski Christoph8,Conte PierFranco2,Hortobagyi Gabriel N.1

Affiliation:

1. a Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA;

2. b Modena University Hospital, Modena, Italy;

3. c Oncology Research and Treatment Center, Ankara University, Ankara, Turkey;

4. d Royal Marsden NHS Foundation Trust & Institute for Cancer Research, London, United Kingdom;

5. e French Cancer National Institute, Paris, France;

6. f German Breast Group, Neu-Isenburg, Germany;

7. g Hospital Universitario Gregorio Marañon, Madrid, Spain;

8. h Medical University-General Hospital, Vienna, Austria

Abstract

Abstract Significant advances in the treatment of patients with breast cancer have been made in the past 10 years. The current systemic treatment of breast cancer is characterized by the discovery of multiple cancer targets leading to treatments that are more sophisticated and specific than conventional cytotoxic chemotherapy. Two classes of compounds that have helped improve clinical outcomes are small molecules and monoclonal antibodies targeting specific tyrosine kinase receptors. Many novel targets have been discovered, and parallel multiple approaches to anticancer therapy have recently emerged from the literature. One promising strategy is targeting the proangiogenic vascular endothelial growth factors (VEGFs), either by ligand sequestration (preventing VEGF receptor binding) or inhibiting downstream receptor signaling. Bevacizumab, a monoclonal antibody directed against VEGF, has been shown to improve the efficacy of taxanes in frontline treatment of patients with metastatic breast cancer. This review outlines the most promising breast cancer studies using bevacizumab combined with traditional cytotoxic agents in advanced breast cancer. In addition, we discuss the current indications reviewed by the Oncologic Drug Advisory Committee and define our vision of how the benefit of patient clinical trials should be measured.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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